New compounds: Synthesis of 2‐chloromethylbenzo[b]furans

Wayne K. Anderson; Jeffrey C. Bottaro; Michael J. Halat

doi:10.1002/jps.2600690238

New compounds: Synthesis of 2‐chloromethylbenzo[b]furans

Wayne K. Anderson
, Jeffrey C. Bottaro
, Michael J. Halat

Pharmaceutical Sciences

SUNY Buffalo

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

Abstract

2‐Chloromethylbenzo[b]furans were prepared in high overall yield from the corresponding chloroethylphenyl ethers through chloroepoxide and α‐chlorophenylacetone intermediates.

Original language	English
Pages (from-to)	232-233
Number of pages	2
Journal	Journal of Pharmaceutical Sciences
Volume	69
Issue number	2
DOIs	https://doi.org/10.1002/jps.2600690238
State	Published - Feb 1980

Keywords

2‐Chloromethylbenzo[b]furans—synthesis
Benzo[b]furans—synthesis of 2‐chloromethyl compounds
Heterocycles—synthesis of 2‐chloromethylbenzo[b]furans

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10.1002/jps.2600690238

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@article{051024e85944453aa543214830524b0e,

title = "New compounds: Synthesis of 2‐chloromethylbenzo[b]furans",

abstract = "2‐Chloromethylbenzo[b]furans were prepared in high overall yield from the corresponding chloroethylphenyl ethers through chloroepoxide and α‐chlorophenylacetone intermediates.",

keywords = "2‐Chloromethylbenzo[b]furans—synthesis, Benzo[b]furans—synthesis of 2‐chloromethyl compounds, Heterocycles—synthesis of 2‐chloromethylbenzo[b]furans",

author = "Anderson, \{Wayne K.\} and Bottaro, \{Jeffrey C.\} and Halat, \{Michael J.\}",

year = "1980",

month = feb,

doi = "10.1002/jps.2600690238",

language = "English",

volume = "69",

pages = "232--233",

journal = "Journal of Pharmaceutical Sciences",

issn = "0022-3549",

publisher = "Elsevier B.V.",

number = "2",

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TY - JOUR

T1 - New compounds

T2 - Synthesis of 2‐chloromethylbenzo[b]furans

AU - Anderson, Wayne K.

AU - Bottaro, Jeffrey C.

AU - Halat, Michael J.

PY - 1980/2

Y1 - 1980/2

N2 - 2‐Chloromethylbenzo[b]furans were prepared in high overall yield from the corresponding chloroethylphenyl ethers through chloroepoxide and α‐chlorophenylacetone intermediates.

AB - 2‐Chloromethylbenzo[b]furans were prepared in high overall yield from the corresponding chloroethylphenyl ethers through chloroepoxide and α‐chlorophenylacetone intermediates.

KW - 2‐Chloromethylbenzo[b]furans—synthesis

KW - Benzo[b]furans—synthesis of 2‐chloromethyl compounds

KW - Heterocycles—synthesis of 2‐chloromethylbenzo[b]furans

UR - https://www.scopus.com/pages/publications/0018888896

U2 - 10.1002/jps.2600690238

DO - 10.1002/jps.2600690238

M3 - Article

C2 - 7359338

AN - SCOPUS:0018888896

SN - 0022-3549

VL - 69

SP - 232

EP - 233

JO - Journal of Pharmaceutical Sciences

JF - Journal of Pharmaceutical Sciences

IS - 2

ER -

New compounds: Synthesis of 2‐chloromethylbenzo[b]furans

Abstract

Keywords

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